Ligand-Induced Variations in Symmetry and Structural Dimensionality of Lead Oxide Carboxylates

Abstract

Four new lead oxide carboxylates have been prepared through solvothermal reactions between lead oxide and substituted benzoic acids. In these extended inorganic hybrids, edge-sharing Pb4O tetrahedra form 1-D inorganic substructures that are further coordinated by the carboxylate ligands. In two isostructural phases, Pb2O(C7H4(CH3)O2)2·0.25(H2O) and Pb2O(C7H4BrO2)2·0.23(C2H5OH), distorted Pb4O tetrahedra produce helical Pb2O2+ chains. The 1-D chains in these structures are coordinated by p-toluate and 4-bromobenzoate ligands, respectively. Right- and left-handed helices are related through inversion, and the structures crystallize in the centrosymmetric I41/a space group. In Pb2O(C7H4O3), linear Pb2O2+ chains are linked into 2-D layers by salicylate ligands, resulting in the achiral, polar space group Fdd2. In Pb3O2(C7H3FO3)·0.71(H2O), linear Pb3O22+ double chains are linked into layers by 4-fluorosalicylate ligands. The compound crystallizes in the chiral, noncentrosymmetric space group P21. For each of the ligands in the new structures as well as in four previously reported structures, a ratio of the noncoordinating to coordinating volumes has been calculated. This ligand volume ratio shows a clear inverse correlation with the overall dimensionality of the lead oxide carboxylates. The analysis encompasses 1- to 3-D structures and ligands of differing denticities. Structures were determined through single-crystal X-ray diffraction, and the new compounds were further characterized via powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, and elemental analysis.

Publisher

American Chemical Society

Publication Date

4-5-2017

Publication Title

Crystal Growth & Design

Department

Chemistry and Biochemistry

Document Type

Article

DOI

10.1021/acs.cgd.6b01558

Language

English

Format

text

Link to Full Text

Share

COinS